Canonical Allele Identifier: CA517048367

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66931407A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711565A>C , CM000685.2:g.67711565A>C	GRCh38
NC_000023.10:g.66931407A>C , CM000685.1:g.66931407A>C	GRCh37
NC_000023.9:g.66848132A>C	NCBI36
NG_009014.2:g.172534A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*397A>C	ENSP00000379358.4:n.*397A>C
ENST00000374690.9:c.2049A>C MANE Select	ENSP00000363822.3:p.Pro683=
ENST00000396043.3:c.676A>C	ENSP00000379358.3:n.676A>C
ENST00000396044.8:c.2049A>C	ENSP00000379359.3:p.Pro683=
ENST00000612452.5:c.2049A>C	ENSP00000484033.2:p.Pro683=
ENST00000374690.7:c.2049A>C	ENSP00000363822.3:p.Pro683=
ENST00000396043.2:c.453A>C	ENSP00000379358.2:p.Pro151=
ENST00000396044.7:c.2049A>C	ENSP00000379359.3:p.Pro683=
ENST00000612452.4:c.1479A>C	ENSP00000484033.1:p.Pro493=
NM_000044.3:c.2049A>C	NP_000035.2:p.Pro683=
NM_001011645.2:c.453A>C	NP_001011645.1:p.Pro151=
NM_000044.4:c.2049A>C	NP_000035.2:p.Pro683=
NM_001011645.3:c.453A>C	NP_001011645.1:p.Pro151=
NM_000044.6:c.2049A>C MANE Select	NP_000035.2:p.Pro683=